Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 67562-20-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Isobutyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane delivers a sterically shielded boronate ester with enhanced stability and moisture tolerance. This bench-stable reagent integrates readily into Suzuki-Miyaura coupling protocols, enabling efficient carbon–carbon bond formation under mild conditions. The isobutyl substituent provides optimal reactivity balance, while the tetramethyl groups confer resistance to protodeboronation.
2-Isobutyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent for Suzuki-Miyaura cross-coupling reactions. Its sterically protected boronate moiety enables high functional group tolerance and reliable coupling with aryl, heteroaryl, and vinyl halides under mild conditions. The isobutyl substituent enhances solubility and stability, facilitating purification and scalable synthesis of complex molecular architectures.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: